|
HS Code |
767711 |
| Chemicalname | Iodine Bromide |
| Chemicalformula | IBr |
| Molarmass | 206.808 g/mol |
| Appearance | Red-brown solid |
| Odor | Pungent |
| Meltingpoint | 42°C |
| Boilingpoint | 116°C |
| Density | 4.6 g/cm³ |
| Solubilityinwater | Reacts |
| Casnumber | 7789-33-5 |
As an accredited Iodine Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle labeled "Iodine Bromide," featuring hazard symbols, tamper-evident seal, and detailed safety instructions. |
| Shipping | Iodine bromide (IBr) should be shipped in tightly sealed, corrosion-resistant containers under cool, dry conditions. It is classified as a hazardous material due to its corrosive and oxidizing properties. Proper labeling, documentation, and compliance with relevant transportation regulations, such as UN 2289, are essential for safe shipping and handling. |
| Storage | Iodine bromide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from light. It must be kept separate from incompatible substances such as strong reducing agents and organic materials. Use non-reactive materials like glass for storage. Properly label the container and ensure it is protected from moisture and direct sunlight to maintain its stability. |
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Purity 99%: Iodine Bromide with 99% purity is used in organic synthesis processes, where it ensures high reaction yield and product consistency. Molecular Weight 206.8 g/mol: Iodine Bromide at a molecular weight of 206.8 g/mol is used in halogen exchange reactions, where it enables precise stoichiometric conversions. Melting Point 42°C: Iodine Bromide with a melting point of 42°C is used in low-temperature chemical manufacturing, where it facilitates handling and controlled reactivity. Stability Temperature up to 100°C: Iodine Bromide stable up to 100°C is used in pharmaceutical intermediate synthesis, where it maintains chemical integrity and minimizes decomposition. Fine Particle Size <50 µm: Iodine Bromide with particle size below 50 µm is used in catalysis applications, where it achieves rapid dissolution and homogenous mixing. Reagent Grade: Iodine Bromide of reagent grade is used in analytical chemistry settings, where it guarantees purity and precise analytical results. Aqueous Solubility 12 g/100 mL: Iodine Bromide with aqueous solubility of 12 g/100 mL is used in solution-based extraction processes, where it enhances solute recovery and process efficiency. |
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Bumping into Iodine Bromide outside of a university lab seems unlikely, but this copper-colored compound has a knack for making its way into a surprising range of places. Known by its formula, IBr, Iodine Bromide lands somewhere between its better-known relatives—iodine chloride and the smartly packaged bromine chloride. For a long time, chemists only gave it passing mention. These days, folks working with specialty syntheses or industrial-scale halogenation give it a second glance. The lure comes from a simple equation: better control during synthesis often brings better product yield and cleaner results, and Iodine Bromide brings just the right temperament to make that equation work out more reliably.
Take a look at the numbers for Iodine Bromide and it becomes clear why practitioners still order it, despite cheaper or more common halides on the market. Weighted at a molecular mass of about 206.8 g/mol, it stands out for delivering a neat, stoichiometric punch without much fuss during mixing or reaction. People in the know appreciate its melting point, which hovers just below room temperature—usually between 40 and 42°C. That 'soft solid at room temp' performance separates it from others who stubbornly remain granular or evaporate too soon, often complicating containment or process flow. In storage, Iodine Bromide’s somewhat volatile nature keeps everyone alert. A well-sealed bottle, handled with gloves, stays stable, but leave the cap loose and you’ll start to pick up a whiff of that strong, biting odor characteristic of halogens working together. It's this mixture of reliability and easy activation that gives it practical value over pure iodine or bromine for many users.
Anyone who has ever worked with elemental iodine in the lab—those heavy, dark crystals—knows that it’s not always pleasant trying to get a clean reaction. Bromine isn’t much better: an aggressive, reddish-brown liquid that leaves persistent stains and rarely plays nice with glassware. Iodine Bromide, by contrast, acts almost gentle, a product of two strong personalities finding common ground. It melts and blends without splitting into layers or sending fumes skyward. Users credit its intermediate reactivity: strong enough to facilitate halogenation reactions in organic synthesis, but less likely to trigger violent outbursts or unwanted side reactions that can haunt a chemist for hours. There’s no dodging safety procedures—halides always demand respect—but Iodine Bromide’s balanced nature draws attention from those aiming for high-precision results. It lets syntheses run to completion without unwanted surprises, helping labs minimize waste or rework costs.
I got my hands dirty with halogen compounds back in graduate school. Most folks outside chemistry circles may never need to think about halides at all, but in chemical manufacturing, dye synthesis, and advanced electronics, compounds like Iodine Bromide matter. People designing novel organic syntheses often struggle with selectivity—choosing the right compound to introduce a halogen atom just so. Iodine Bromide offers a ‘Goldilocks’ solution for certain aromatics and hydrocarbons; it slides into reactions smoothly, not too fast, not too slow. Think pharmaceutical precursors, where tiny changes in reactivity net big differences in product quality. Or the thin films used for optical coatings and detectors, where every trace contaminant can spell disaster. Even in analytical work, where reference standards need purity and predictable reactivity, Iodine Bromide often finds favor over the messier alternatives.
No compound solves all problems, and Iodine Bromide brings its own set of limitations to the table. Its tendency to react with water, releasing both halogens (and sometimes a lingering acidic smell), means storage always calls for caution. Chemists avoid unnecessary moisture and prepare to neutralize small spills with the same care as they would for bromine or iodine. Shipping regulations treat Iodine Bromide with healthy suspicion—one reason you don’t spot it in general stores or amateur setups. Handling those safety demands is just part of the cost for anyone set on using this compound. Comparing it against chlorine-based halides or modern catalytic reagents, you’ll notice the cost and regulatory burden usually runs higher. But for certain syntheses that absolutely require predictable halogen behavior, these trade-offs fall in Iodine Bromide’s favor.
Anyone reading spec sheets for halogen compounds soon gets lost in tables and purity figures. In the field, working with Iodine Bromide feels different from juggling flasks of bromine or picking through caked, gray iodine. A lot depends on the speed at which it dissolves, its ability to react cleanly, and the lack of precipitate or unwanted byproducts afterward. In organic reactions, this lands as tangible time saved and fewer headaches. Years spent preparing N-substituted aromatic compounds taught me to respect that consistency. Instead of poking around with multiple purification cycles, a well-timed Iodine Bromide reaction often asked for less cleanup. Compare that to wrestling with bromine gas or the endless vapor stains of chlorine and the practical value starts to show up right on the balance sheet. It’s this boots-on-the-ground performance, not just numbers, that keeps specialty buyers coming back despite the price.
Working with halogens today means more than just getting the chemistry right. Environmental rules have tightened around many specialty chemicals, especially halides with a taste for corrosion and atmospheric release. Iodine Bromide doesn’t present the same ozone issues as raw bromine or chlorine, but users still track disposal closely. Waste that mixes with water needs special handling to avoid releasing free halogens or generating hazardous acids. In decades past, disposal practices could get lax. Thankfully, industry practice and oversight have both sharpened—closed systems, strong ventilation, and neutralization protocols now form standard operating procedure almost everywhere. Tighter controls affect price and sourcing, but the payoff comes through safer workplaces and cleaner communities. Both academics and industrial users adjust by ordering only what they need, double-checking storage, and building secondary containment right into daily workflows.
For anyone tasked with purchasing specialty halides, Iodine Bromide ends up competing with a global collection of compounds, each boasting its own blend of reactivity and price. Companies focus not just on purity—often listed at 99 percent or greater—but how consistently the lot performs batch to batch. Unlike mass-market reagents or simple salts, Iodine Bromide attracts buyers looking for reliability and precision. Its cost reflects that niche demand, with smaller-scale packaging and tighter quality controls taking precedent. Markets sometimes see periodic shortages tied to fluctuations in halogen production. When bromine or iodine prices spike, Iodine Bromide rides along, a reminder of its reliance on those base elements. Competitive alternatives crop up in academia, but few match its blend of predictable reactivity and clean separation in practice. Buyers in electronics, pharmaceuticals, or dye development return again and again for the same reason: results justify the expense when batch losses or contamination would cripple profitability or slow down a product launch.
Research labs constantly search for cleaner, more controllable ways to introduce halogen atoms into complex molecules. Iodine Bromide, with its intermediate reactivity, wins praise in fine chemical synthesis and pharmaceutical prep. Chemists find that it frequently produces less waste compared to stronger oxidizers, and because its reactions can be stopped and restarted without massive side product formation, experiments move with less risk of failure. Those working with aromatic substitutions or heteroatom halogenation highlight Iodine Bromide’s ability to gently nudge a substrate without bulldozing surrounding functional groups. Technology shifts mean even small gains in selectivity or reaction simplicity open new doors. In my own work, switching to Iodine Bromide often solved stubborn yield issues—no need to clean glassware endlessly or fight off clouds of elemental halogen. That practical know-how, passed down through graduate labs and industrial teams, turns into faster R&D and more predictable scale-up when projects jump from benchtop to pilot plant.
Learning to handle Iodine Bromide safely never leaves you, even years out of the lab. Old habits—double-glove use, face shields, dryboxes—live on for good reason. At the same time, better practices have shaped how new chemists work. Suppliers now highlight low-contamination storage vessels and improved transfer techniques. Standardized training pushes safe handling well beyond a quick brush-up on safety data sheets: users check for corrosion, keep emergency absorbents close at hand, and never compromise on fresh air. Educators know that most accidents don’t come from explosive mistakes but from small slips in routine, so the best labs layer in redundancy and regular review. Rather than see these steps as obstacles, teams take pride in a track record of safe, unremarkable use. A culture of respect and training around Iodine Bromide and related reagents becomes its own solution, smoothing out the risk curve while keeping doors open for innovation in lab and factory alike.
For all its benefits, Iodine Bromide still comes wrapped in practical challenges. Regulations tighten year by year, and raw material costs swing with international supply lines. Decision-makers inside chemical supply chains take these uncertainties into account, building flexibility into sourcing and pricing agreements. Some labs have started to experiment with in situ generation of Iodine Bromide, mixing iodine and bromine together just before use to cut down on storage hazards. This shift demands more rigorous process control, and for now, most users prefer the predictability of buying pre-mixed, quality-assured material. Still, as new tools and monitoring systems reach the industry, the balance may tip. Improved packaging technologies and smarter storage trackers already make a difference, letting users spot leaks or slow degradation long before waste turns into a full-blown safety problem. The long-term goal stays the same: keep the benefits of precision halogenation without letting risk outpace reward.
In labs and factories worldwide, Iodine Bromide quietly stakes its claim as a specialty halide for those who value precision and reliability over brute strength or lowest price. Its middle-of-the-road reactivity translates to meaningful improvements for practitioners, whether the task involves building advanced dyes, tuning electronic components, or prepping fine pharmaceuticals. For all its hazards, its well-understood behavior makes it a trustworthy component for people who know what they’re doing. As the regulatory environment evolves, suppliers and users both commit to more robust safety and handling routines. That cycle of experience, risk reduction, and technical refinement keeps Iodine Bromide in play long after other compounds fall out of favor. Future breakthroughs may yet offer cheaper or safer substitutes, but right now, for those who count on predictable, controllable halogenation, Iodine Bromide answers the call.